ENST00000698420.1:c.*1152A>T
(TAP1)
|
ENSP00000513708.1:n.*1152A>T
|
|
ENST00000698421.1:c.*894A>T
(TAP1)
|
ENSP00000513709.1:n.*894A>T
|
|
ENST00000698422.1:c.1811A>T
(TAP1)
|
ENSP00000513710.1:p.Asp604Val
|
|
ENST00000698423.1:c.2000A>T
(TAP1)
|
ENSP00000513711.1:p.Asp667Val
|
|
ENST00000698424.1:c.1871A>T
(TAP1)
|
ENSP00000513712.1:p.Asp624Val
|
|
ENST00000354258.5:c.2000A>T
(TAP1)
MANE Select
|
ENSP00000346206.5:p.Asp667Val
|
|
ENST00000643049.2:c.545A>T
(TAP1)
|
ENSP00000494148.2:p.Asp182Val
|
|
ENST00000643923.1:n.1436A>T
(TAP1)
|
|
|
ENST00000645078.1:n.1595A>T
(TAP1)
|
|
|
ENST00000354258.4:c.2180A>T
(TAP1)
|
ENSP00000346206.4:p.Asp727Val
|
|
ENST00000395330.5:c.-10+2834T>A
(PSMB9)
|
ENSP00000378739.1:n.-10+2834T>A
|
|
ENST00000414474.5:c.-10+2238T>A
(PSMB9)
|
ENSP00000394363.1:n.-10+2238T>A
|
|
ENST00000486332.1:n.1925A>T
(TAP1)
|
|
|
ENST00000487296.1:n.880A>T
(TAP1)
|
|
|
NM_000593.5:c.2180A>T
(TAP1)
|
NP_000584.2:p.Asp727Val
|
|
NM_001292022.1:c.1397A>T
(TAP1)
|
NP_001278951.1:p.Asp466Val
|
|
NM_001292022.2:c.1397A>T
(TAP1)
|
NP_001278951.1:p.Asp466Val
|
|
NM_000593.6:c.2000A>T
(TAP1)
MANE Select
|
NP_000584.3:p.Asp667Val
|
|